Clinical Research Associate

JR Italy; Sassari; In loco; EUR 30.000 - 60.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking skilled Clinical Research Associates (CRAs) to join their expanding team. This role focuses on ensuring the timely and quality delivery of site monitoring activities for a global study. Candidates should possess a solid background in clinical research, particularly in site monitoring, with a strong understanding of ICH GCP and relevant regulations. The company offers a dynamic environment where your commitment to quality and adherence to timelines will directly contribute to project success. If you're looking to make a significant impact in clinical research, this opportunity is perfect for you.

Competenze

• 1-4 years of experience in site monitoring within clinical research.
• Strong understanding of ICH GCP and clinical trial regulations.

Mansioni

• Deliver on the Site Monitoring Plan ensuring adherence to quality standards.
• Assist in identifying new potential sites across various therapeutic areas.

Conoscenze

Site Monitoring

ICH GCP

Verbal Communication

Written Communication

Multitasking

Formazione

Bachelor's degree in a scientific discipline

Master's degree in a scientific discipline

Descrizione del lavoro

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CliniRx has a number of CRA positions available to support a global study in Q1 2025.

We are expanding rapidly and have multiple permanent opportunities to join us on a global study. Ideally, candidates will come from a CRO background with experience across various therapeutic areas.

As a global contract research organization (CRO), we offer a diverse range of clinical development and resource solutions, including full-service CRO and functional service provider (FSP) models. We support clinical outsourcing needs for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises facing unique challenges. Our presence includes key markets such as the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.

Primary Purpose:

We are seeking skilled CRAs to ensure the timely and quality delivery of site monitoring activities in line with our Site Monitoring Plan (SMP).

Key Responsibilities:

1. Deliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality standards and timelines.
2. Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.
3. Site Identification: Assist in identifying new potential sites across various therapeutic areas to expand our clinical network.
4. Continuous Skill Development: Regularly improve technical and soft skills to enhance performance and project outcomes.

Work Relations:

• Report to the Manager of Clinical Operations regarding project, functional, and administrative matters.
• Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff.

Value Added:

Your commitment to quality and adherence to timelines is crucial for the efficient delivery of our projects and overall success.

Key Success Factors:

• Timely and high-quality execution of site monitoring activities.
• Prompt report generation and submission to stakeholders.
• Education: Bachelor’s or Master’s degree in a scientific discipline.
• Experience: 1-4 years in site monitoring within clinical research.
• Skills: Strong understanding of ICH GCP and relevant clinical trial regulations; excellent verbal and written communication skills; ability to multitask and work effectively under demanding timelines.